N-Carbethoxy-4-tropinone
N-Carbethoxy-4-tropinone Basic information
- Product Name:
- N-Carbethoxy-4-tropinone
- Synonyms:
-
- n-(carboethoxy)tropinone
- 3-Oxo-8-azabicylo[3.2.1]octane-8-carboxylic acid
- ethyl 3-oxo-8-azabicyclo(3.2.1)octane-8-carboxylate
- N-(Carboethoxy)tropinone~3-Oxo-8-azabicyclo[3.2.1]octane-8-carboxylic acid ethyl ester
- N-ethoxycarbonylnortropan-3-one
- N-(Ethoxycarbonyl)tropinone,99%
- N-(ETHOXYCAZBONYL)NORTROPINONE
- N-(Ethoxycarbonyl)nortropinone, 99%
- CAS:
- 32499-64-2
- MF:
- C10H15NO3
- MW:
- 197.23
- EINECS:
- 1312995-182-4
- Product Categories:
-
- Miscellaneous Biochemicals
- Mol File:
- 32499-64-2.mol
N-Carbethoxy-4-tropinone Chemical Properties
- Boiling point:
- 152-153°C 11mm
- Density
- 1.1575 (rough estimate)
- refractive index
- 1.4876-1.4896
- Flash point:
- 152-153°C/11mm
- storage temp.
- Sealed in dry,Room Temperature
- pka
- -1.66±0.20(Predicted)
- form
- Liquid
- color
- Clear slightly yellow to light brown
- BRN
- 1530944
- CAS DataBase Reference
- 32499-64-2(CAS DataBase Reference)
Safety Information
- Safety Statements
- 24/25
- HS Code
- 29399990
N-Carbethoxy-4-tropinone Usage And Synthesis
Chemical Properties
CLEAR SLIGHTLY YELLOW TO LIGHT BROWN LIQUID
Synthesis
532-24-1
541-41-3
32499-64-2
To a dry 500 mL round-bottomed flask were added a stirrer, 8-methyl-8-azabicyclo[3.2.1]octan-3-one (10.0 g, 0.072 mol) and potassium carbonate (0.050 g). Anhydrous toluene (90 mL) was added, followed by slow dropwise addition of ethyl chloroformate (21 mL, 0.22 mol) via syringe. A condenser tube and nitrogen bubbler were installed and the reaction was heated to reflux with stirring overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure and the resulting brown oil was dissolved in dichloromethane (100 mL) and washed with water (100 mL). The organic and aqueous layers were separated in a partition funnel and the aqueous layer was extracted with dichloromethane (3 x 50 mL). The organic phases were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane, 1:3) to afford ethyl 3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylate (13.1 g, 92% yield) as a light yellow oil.1H NMR (δ): 4.51 (br s, 2H), 4.16 (q, J = 7.2 Hz, 2H), 2.63 (br s , 2H), 2.31 (dd, J = 17.4, 1.6 Hz, 2H), 2.07-2.03 (m, 2H), 1.65 (d, J = 7.6 Hz, 2H), 1.25 (t, J = 7.2 Hz, 3H).13C NMR (δ): 208.3, 154.1, 61.6, 53.2, 49.1, 29.5 (2), 28.8 (2), 14.8 (2), 28.8 (2), 29.5 (2), 29.5 (2), 28.8 (2), 28.8 (2), 28.8 (2), 29.5 (2) 28.8 (2), 14.9.
References
[1] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 4, p. 629 - 632
[2] Journal of Heterocyclic Chemistry, 2004, vol. 41, # 4, p. 569 - 574
[3] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 24, p. 7551 - 7558
[4] Patent: CN105294674, 2016, A. Location in patent: Paragraph 0147; 0148; 0149
[5] Patent: WO2018/140876, 2018, A1. Location in patent: Page/Page column 216
N-Carbethoxy-4-tropinoneSupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 4006356688 18621169109
- market03@meryer.com
- Tel
- 400-6106006
- saleschina@alfa-asia.com
- Tel
- 021-67121386
- Sales-CN@TCIchemicals.com
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
N-Carbethoxy-4-tropinone(32499-64-2)Related Product Information
- Tris(trimethylsilyl)phosphate
- N-Carbobenzyloxyglycine
- N-OCTANE
- Oxyfluorfen
- 3-Nitroacetophenone
- Ethylparaben
- Oxygen-fluorine acid
- Tropinone
- Tropisetron hydrochloride
- Ethanol
- Tropisetron
- Levofloxacin carboxylic acid
- Ethyl acetate
- Acetophenone
- (1R,3s,5S)-3-(3-Isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octane
- Diethyl ether
- N-Boc-Nortropinone
- Cycloheptanone